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CODEX: a normalization and copy number variation detection method for whole exome sequencing

High-throughput sequencing of DNA coding regions has become a common way of assaying genomic variation in the study of human diseases. Copy number variation (CNV) is an important type of genomic variation, but detecting and characterizing CNV from exome sequencing is challenging due to the high leve...

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Bibliografski detalji
Izdano u:Nucleic Acids Res
Glavni autori: Jiang, Yuchao, Oldridge, Derek A., Diskin, Sharon J., Zhang, Nancy R.
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2015
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4381046/
https://ncbi.nlm.nih.gov/pubmed/25618849
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gku1363
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